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- 1.
- 2.
For a review gathering some examples of this type of reaction see: [9].
- 3.
With Pt(IV): [10].
- 4.
With cationic Au(I): [11].
- 5.
Sames also invoked the possibility of a platinum vinylidene, see Ref. [10].
- 6.
See also Ref. [21].
- 7.
However, as discussed in Chap. 1, Sect. 1.5.1, formation of 53 can also arise from a 1,2-OAc shift/cyclopropanation sequence, but it was not evoked by the authors.
- 8.
See also: [37 ].
- 9.
For a study where prenyl double bonds showed distinct behaviors, see Ref. [38 ].
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Simonneau, A. (2014). New Advances in the Gold-Catalyzed Cycloisomerization Reactions of Enynes: 1,5-hydride Shifts and Access to Ketomacrolactones. In: Gold-Catalyzed Cycloisomerization Reactions Through Activation of Alkynes. Springer Theses. Springer, Cham. https://doi.org/10.1007/978-3-319-06707-0_2
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